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      Molecular Research on Emerging Viruses: Evolution, Diagnostics, Pathogenesis, and Therapeutics

      editorial
      1 , 2 , 3 , 4
      International Journal of Molecular Sciences
      MDPI

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          Abstract

          Editorial Viruses are increasingly recognized as emerging infectious disease agents in both humans and animals. Zoonotic viruses, in particular, often evolve rapidly to adapt to new hosts with enhanced virulence and emerge or re-emerge to cause epidemics. Factors such as urbanization, global warming, and dense human and animal populations may have contributed to the emergence of some viruses. The recent epidemics caused by Zika virus and Middle East respiratory syndrome coronavirus (MERS-CoV) clearly illustrate the ability of emerging viruses to pose huge public health problems within a short time. Much more research effort is needed to understand the evolution and pathogenesis of these emerging viruses, as well as the development of diagnostics and therapeutics to combat existing and future epidemics. Recent advances in molecular techniques, such as sequencing and metagenomics, have accelerated our understanding of genetic and host diversity of emerging viruses, and hence their evolutionary pathways. Nevertheless, many questions remain unanswered. For example, while severe acute respiratory syndrome coronavirus (SARS-CoV) was originated from horseshoe bats as the primary reservoir [1,2], the ancestral origin of MERS-CoV has not been ascertained yet despite its close relationship with some bat coronaviruses [3,4,5]. Molecular assays play a crucial role in the diagnosis of emerging viruses such as Zika virus, which may overcome the limitations of viral cultures and serological tests, allowing more convenient, rapid, and accurate diagnosis. Immense research efforts have also been recently made to reveal the diverse virulence mechanisms and host–pathogen interactions of emerging viruses. On the other hand, with only a few exceptions such as influenza virus, treatment of emerging viruses is mostly supportive, as a result of the lack of effective antivirals for most of these viruses. Discovery of novel antiviral agents is eagerly awaited for many emerging viruses, though identification of antiviral targets which spare the host replication machinery can be difficult. Therefore, new research directions are crucial to predict, prevent, and combat virus diseases. In this special issue, “Molecular Research on Emerging Viruses: Evolution, Diagnostics, Pathogenesis, and Therapeutics”, insights into advances and discoveries in understanding the different aspects of various emerging viruses are given by eight original studies and four review articles. Three articles focus on arthropod-borne viruses (arboviruses) which are important emerging pathogens having caused various epidemics in recent years. In the systematic review and meta-analysis study by Coelho et al., the prevalence of microcephaly in infants born to Zika virus-infected women among all pregnancies was estimated [6], which may contribute to the understanding of the public health impact of this emerging arbovirus. The article by Le Coupanec et al., studies the viral replication during co-infection of Chikungunya and Dengue viruses which has been observed in some patients [7]. Co-infection with both viruses in Aedes aegypti mosquitoes was found to facilitate viral replication, suggesting the importance of pathogen–pathogen interactions. In another article, Lu et al. investigated the antiviral activity of histone deacetylase (HDAC) inhibitors as host-targeting agents against Japanese encephalitis virus (JEV) [8]. Tubacin, a selective HDAC6 inhibitor was found to be a potential host-targeting agent, demonstrating preventive and therapeutic activities against JEV infection. Zoonotic influenza viruses remain a significant concern to both human health and food industry, with their tendency to re-assort and mutate to generate novel strains capable of interspecies transmission. Yet, it remains difficult to predict the emergence potential of new strains. In the article by Eng et al., a machine learning approach was taken to build a zoonotic strain prediction model which could classify avian, human, or zoonotic strains with an estimated zoonotic risk [9]. In another article, Zhang et al. investigated the role of swine cellular microRNAs in regulating swine pandemic H1N1/2009 influenza A virus (SIV-H1N1/2009) replication [10]. Two microRNAs, ssc-miR-204 and ssc-miR-4431, were found to target viral haemagglutinin (HA) and non-structural protein (NS), respectively, and inhibit viral replication, providing insights into virus–host interaction and control of the virus in swine population. Hepatitis viruses pose significant disease burdens worldwide and some have emerged or re-emerged in different populations. In the review article by Sridhar et al., the genotypic diversity and evolution of existing hepatitis E virus strains are reviewed, with a special focus on the emergence of camel hepatitis E variants [11]. In another article, Lee et al. reported novel hepatitis B virus intergenotypic recombinants from a patient co-infected with genotype A2 and C2 [12]. The results may prompt further studies on the clinical implications of such novel recombinant virus strains. Coronaviruses have continued to emerge or re-emerge in the last two decades to cause epidemics in humans and animals. In the review article by Lin et al., current knowledge on the molecular evolution, pathogenicity, and epidemiology of infectious bronchitis virus, which poses huge economic threats to poultry farms worldwide, was summarized [13]. Enteroviruses are another group of emerging viruses that can cause severe sporadic infections or epidemics especially in young children. In particular, enterovirus-D68 has emerged in recent years in various countries and is increasingly recognized as an important respiratory pathogen in the young and immunocompromised. In the article by Yip et al., the first fatal case of EV-D68 infection and genetic diversity of EV-D68 strains in Hong Kong were described [14]. The study also found a newly emerged subclade B3 and an interclade recombination between clade A and D2 strains in China. Two articles report on the virus–host interaction during porcine reproductive and respiratory syndrome virus (PRRSV) infection which causes severe losses in the swine industry worldwide. In one article, Ji et al. describes the role of porcine interferon stimulated gene 12a (ISG12A) in restricting PRRSV replication [15]. ISG12A was found to be upregulated in cells or tissues of pigs and could suppress PRRSV replication in infected MARC-145 cells, supporting its role in host immune response to PRRSV. In another article, Liang et al. describes the transcriptomic differences in porcine alveolar macrophages from two different pig breeds, Tongcheng and Large White pigs, in response to PRRSV infections [16]. Transcriptomics profiling of infected macrophages suggested that Tongcheng pigs, being more resistant to PRRSV infection, may promote the extravasation and migration of leukocytes from the capillaries to the surrounding tissues to defend against PRRSV and suppress apoptosis of macrophages in order to enhance antigen presentation. Last but not least, some mammalian arenaviruses are emerging viruses that may infect humans to cause lethal hemorrhagic fever. In the article by Ly, current knowledge on the differential immune responses to arenaviruses were summarized, which may help understand their pathogenesis and contribute to the development of vaccines [17].

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          Most cited references15

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          • Article: not found

          Isolation of a novel coronavirus from a man with pneumonia in Saudi Arabia.

          A previously unknown coronavirus was isolated from the sputum of a 60-year-old man who presented with acute pneumonia and subsequent renal failure with a fatal outcome in Saudi Arabia. The virus (called HCoV-EMC) replicated readily in cell culture, producing cytopathic effects of rounding, detachment, and syncytium formation. The virus represents a novel betacoronavirus species. The closest known relatives are bat coronaviruses HKU4 and HKU5. Here, the clinical data, virus isolation, and molecular identification are presented. The clinical picture was remarkably similar to that of the severe acute respiratory syndrome (SARS) outbreak in 2003 and reminds us that animal coronaviruses can cause severe disease in humans.
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            Severe acute respiratory syndrome coronavirus-like virus in Chinese horseshoe bats.

            Although the finding of severe acute respiratory syndrome coronavirus (SARS-CoV) in caged palm civets from live animal markets in China has provided evidence for interspecies transmission in the genesis of the SARS epidemic, subsequent studies suggested that the civet may have served only as an amplification host for SARS-CoV. In a surveillance study for CoV in noncaged animals from the wild areas of the Hong Kong Special Administration Region, we identified a CoV closely related to SARS-CoV (bat-SARS-CoV) from 23 (39%) of 59 anal swabs of wild Chinese horseshoe bats (Rhinolophus sinicus) by using RT-PCR. Sequencing and analysis of three bat-SARS-CoV genomes from samples collected at different dates showed that bat-SARS-CoV is closely related to SARS-CoV from humans and civets. Phylogenetic analysis showed that bat-SARS-CoV formed a distinct cluster with SARS-CoV as group 2b CoV, distantly related to known group 2 CoV. Most differences between the bat-SARS-CoV and SARS-CoV genomes were observed in the spike genes, ORF 3 and ORF 8, which are the regions where most variations also were observed between human and civet SARS-CoV genomes. In addition, the presence of a 29-bp insertion in ORF 8 of bat-SARS-CoV genome, not in most human SARS-CoV genomes, suggests that it has a common ancestor with civet SARS-CoV. Antibody against recombinant bat-SARS-CoV nucleocapsid protein was detected in 84% of Chinese horseshoe bats by using an enzyme immunoassay. Neutralizing antibody to human SARS-CoV also was detected in bats with lower viral loads. Precautions should be exercised in the handling of these animals.
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              Comparative analysis of twelve genomes of three novel group 2c and group 2d coronaviruses reveals unique group and subgroup features.

              Twelve complete genomes of three novel coronaviruses-bat coronavirus HKU4 (bat-CoV HKU4), bat-CoV HKU5 (putative group 2c), and bat-CoV HKU9 (putative group 2d)-were sequenced. Comparative genome analysis showed that the various open reading frames (ORFs) of the genomes of the three coronaviruses had significantly higher amino acid identities to those of other group 2 coronaviruses than group 1 and 3 coronaviruses. Phylogenetic trees constructed using chymotrypsin-like protease, RNA-dependent RNA polymerase, helicase, spike, and nucleocapsid all showed that the group 2a and 2b and putative group 2c and 2d coronaviruses are more closely related to each other than to group 1 and 3 coronaviruses. Unique genomic features distinguishing between these four subgroups, including the number of papain-like proteases, the presence or absence of hemagglutinin esterase, small ORFs between the membrane and nucleocapsid genes and ORFs (NS7a and NS7b), bulged stem-loop and pseudoknot structures downstream of the nucleocapsid gene, transcription regulatory sequence, and ribosomal recognition signal for the envelope gene, were also observed. This is the first time that NS7a and NS7b downstream of the nucleocapsid gene has been found in a group 2 coronavirus. The high Ka/Ks ratio of NS7a and NS7b in bat-CoV HKU9 implies that these two group 2d-specific genes are under high selective pressure and hence are rapidly evolving. The four subgroups of group 2 coronaviruses probably originated from a common ancestor. Further molecular epidemiological studies on coronaviruses in the bats of other countries, as well as in other animals, and complete genome sequencing will shed more light on coronavirus diversity and their evolutionary histories.

                Author and article information

                Journal
                Int J Mol Sci
                Int J Mol Sci
                ijms
                International Journal of Molecular Sciences
                MDPI
                1422-0067
                30 January 2018
                February 2018
                : 19
                : 2
                : 398
                Affiliations
                [1 ]State Key Laboratory of Emerging Infectious Diseases, Hong Kong, China; skplau@ 123456hku.hk ; Tel.: +852-22554892; Fax: +852-28551241
                [2 ]Department of Microbiology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China
                [3 ]Carol Yu Centre for Infection, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China
                [4 ]Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China
                Article
                ijms-19-00398
                10.3390/ijms19020398
                5855620
                29385690
                c7a95f17-dd7a-421e-85e7-f3dfd634625c
                © 2018 by the author.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 22 December 2017
                : 26 January 2018
                Categories
                Editorial

                Molecular biology
                Molecular biology

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